Comprehensive variation discovery in single human genomes. - Wikidata - awgldk - TriplyDB

Comprehensive variation discovery in single human genomes.

Comprehensive variation discovery in single human genomes.

http://www.wikidata.org/entity/Q34572388

about

Genetic variation and the de novo assembly of human genomes It's more than stamp collecting: how genome sequencing can unify biological research Evolutionary genomics of epidemic visceral leishmaniasis in the Indian subcontinent Improved genome inference in the MHC using a population reference graph De novo assembly of the Aedes aegypti genome using Hi-C yields chromosome-length scaffolds Genomic analysis and D-xylose fermentation of three novel Spathaspora species: Spathaspora girioi sp. nov., Spathaspora hagerdaliae f. a., sp. nov. and Spathaspora gorwiae f. a., sp. nov.Impact of post-alignment processing in variant discovery from whole exome data Indel variant analysis of short-read sequencing data with Scalpel.ABySS 2.0: resource-efficient assembly of large genomes using a Bloom filter.Comprehensive variation discovery and recovery of missing sequence in the pig genome using multiple de novo assemblies.An improved assembly and annotation of the allohexaploid wheat genome identifies complete families of agronomic genes and provides genomic evidence for chromosomal translocations FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads.Genome-wide profiling of heritable and de novo STR variations.The challenge of small-scale repeats for indel discovery.A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing.Heterozygous genome assembly via binary classification of homologous sequence Best Practices in Insect Genome Sequencing: What Works and What Doesn't.Read clouds uncover variation in complex regions of the human genome.Reducing the search space for causal genetic variants with VASP.The Characteristics of Heterozygous Protein Truncating Variants in the Human Genome.Chromosome-scale shotgun assembly using an in vitro method for long-range linkage An analytical workflow for accurate variant discovery in highly divergent regions.in silico Whole Genome Sequencer & Analyzer (iWGS): A Computational Pipeline to Guide the Design and Analysis of de novo Genome Sequencing Studies.Direct determination of diploid genome sequences.Evaluation of DISCOVAR de novo using a mosquito sample for cost-effective short-read genome assembly.Evolution of the Cytolytic Pore-Forming Proteins (Actinoporins) in Sea Anemones.Transcriptome-based investigation of cirrus development and identifying microsatellite markers in rattan (Daemonorops jenkinsiana).The Genome 10K Project: a way forward.Exome and genome sequencing: a revolution for the discovery and diagnosis of monogenic disorders.Evaluation of the impact of Illumina error correction tools on de novo genome assembly.Genomic innovation for crop improvement.Computational pan-genomics: status, promises and challenges.Comparative analysis of de novo assemblers for variation discovery in personal genomes.Redundans: an assembly pipeline for highly heterozygous genomes SAGE2: Parallel Human Genome Assembly.Detection of long repeat expansions from PCR-free whole-genome sequence data.RecoverY: K-mer based read classification for Y-chromosome specific sequencing and assembly.A 3-way hybrid approach to generate a new high-quality chimpanzee reference genome (Pan_tro_3.0).Population Genomic Analysis of a Pitviper Reveals Microevolutionary Forces Underlying Venom Chemistry.A maternal-effect selfish genetic element in Caenorhabditis elegans.

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Comprehensive variation discovery in single human genomes.

http://www.wikidata.org/entity/Q34572388

description

2014 nî lūn-bûn

@nan

2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Comprehensive variation discovery in single human genomes.

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Comprehensive variation discovery in single human genomes.

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Comprehensive variation discovery in single human genomes.

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type

label

Comprehensive variation discovery in single human genomes.

@ast

Comprehensive variation discovery in single human genomes.

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Comprehensive variation discovery in single human genomes.

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prefLabel

Comprehensive variation discovery in single human genomes.

@ast

Comprehensive variation discovery in single human genomes.

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Comprehensive variation discovery in single human genomes.

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Nature Genetics

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Comprehensive variation discovery in single human genomes.

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Brian Sogoloff

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Carsten Russ

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David B Jaffe

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Diana Tabbaa

http://www.w3.org/2001/XMLSchema#string

Iain MacCallum

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Laurie Holmes

http://www.w3.org/2001/XMLSchema#string

Louise Williams

http://www.w3.org/2001/XMLSchema#string

Neil I Weisenfeld

http://www.w3.org/2001/XMLSchema#string

Ryan Hegarty

http://www.w3.org/2001/XMLSchema#string

Ted Sharpe

http://www.w3.org/2001/XMLSchema#string

P2860

The Sequence of the Human Genome

Finishing the euchromatic sequence of the human genome

An Eulerian path approach to DNA fragment assembly

A map of human genome variation from population-scale sequencing

Efficient de novo assembly of large genomes using compressed data structures

ARACHNE: a whole-genome shotgun assembler

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Integrating common and rare genetic variation in diverse human populations

A framework for variation discovery and genotyping using next-generation DNA sequencing data

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1350-1355

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10.1038/NG.3121

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